XX
Senior Validation QA AssociateQuotient SciencesNottingham, England, United Kingdom
XX

Senior Validation QA Associate

Quotient Sciences
  • GB
    Nottingham, England, United Kingdom
  • GB
    Nottingham, England, United Kingdom
Apply Now

About

Senior Validation QA Associate Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary “Translational Pharmaceutics®” platform integrates Drug Product Manufacturing and Clinical Testing to eliminate silos, reduce costs, improve outcomes, and accelerate drug development times.
Why Join Us Every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.
The Role Senior Validation QA Associate will lead and manage validation projects, maintain documentation, and support continuous improvement initiatives across our Nottingham site. This is a hybrid role with a minimum of 3 days onsite each week.
Key Responsibilities
Lead multi‑functional teams on computer system and equipment validation and qualification, including change management of validated systems.
Ensure validation processes are effective and compliant with regulatory requirements.
Author, review, and approve validation documentation (protocols, reports, incident reports).
Maintain validation records (paper and electronic) and conduct periodic reviews of systems and spreadsheets.
Provide technical validation support and share expertise across the organization.
Support audits and inspections, presenting validation evidence as required.
Drive continuous improvement to reduce risk and enhance efficiency.
Qualifications & Experience
Life Science degree (or equivalent).
Minimum 2 years’ experience in Computer System Validation within a GCP or GMP environment.
Strong communication skills with the ability to collaborate across teams and organizational levels.
Job Demands
High concentration and attention to detail.
Ability to meet strict deadlines and manage multiple tasks simultaneously.
Occasional work outside normal hours to meet client demands.
Compliance with safety procedures in a regulated environment.
Application Requirements Applicants must be aged 18 years or over and not have been debarred by the FDA. Applications from individuals under 18 or who have been debarred will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion Quotient Sciences is committed to fostering an inclusive workplace. We do not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. This policy applies to all aspects of employment, including hiring, promotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr
  • Nottingham, England, United Kingdom

Languages

  • English
Notice for Users

This job comes from a TieTalent partner platform. Click "Apply Now" to submit your application directly on their site.